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Job ID :
43601BR
Location :
US - Kansas - Lenexa
:
Job Description

Key Responsibilities:

  • Review manufacturing documentation for accuracy and completion.
  • Expedite documentation issues to ensure timely release of products.
  • Leads day-to-day activities to ensure swift and accurate completion of product disposition activities.
  • Work closely with the manufacturing, planning, and distribution departments to troubleshoot and solve problems.
  • Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.
  • Assists in tracking departmental metrics and goals.
  • Assist with the training of new personnel.
  • Manage a continuous improvement program within the department.
  • Support all company policies.
  • Performs other duties as assigned.

Minimum Requirements/Qualifications:

  • Possess high school diploma or GED minimum, Associates degree preferred.
  • Course work in the sciences is a plus.
  • Document review experience is preferred.
  • Familiarity with FDA regulations for medical devices is a plus.
  • Possess the ability to manage many tasks and in an organized fashion.
  • Possess proficient computer skills, preferably with experience in Word, Excel and SAP programs.
  • Listen to, and follow, written and verbal instructions.
  • Possess excellent oral and written communication, and problem-solving skills.



Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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